DECIPHER is used by the clinical community to share and compare phenotypic and genotypic data. The DECIPHER database contains data from 51,749 patients who have given consent for broad data-sharing; DECIPHER also supports more limited sharing via consortia.
This is a list of genes for which DECIPHER has open-access patient sequence variants, or DDD research sequence variants. These pages contain information about the genes and their transcripts, matching variants recorded in open-access patients, and associated phenotypes.
The highlighted box on the gene name is a link out to the DECIPHER gene pages and provides collated information extracted from other patients that have openly accessible variants in this gene.
If you are willing for information about you/your child to be entered in DECIPHER please complete and sign the DECIPHER research ethics consent form and return it to your geneticist.
DECIPHER has an advanced search facility that allows querying the database using a combination of terms including phenotypes, gene symbols, chromosomal locations/bands and other fields.
